A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539714



Internal ID20913009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:123334041..126077247hg38UCSC Ensembl
chr2:124091617..126834824hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg382743207
hg192743208
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256705
Samples
Known GenesCNTNAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539714
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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